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PXD040388

PXD040388 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleCD31 defines a subpopulation of human adipose-derived regenerative cells with potent angiogenic properties
DescriptionA major challenge in realizing regenerative treatment using freshly isolated Adipose Derived Regenerative Cells (ADRCs) is the cellular heterogeneity and donor variability. Ex vivo expanded ADRCs (=ASCs) are available at larger quantities and represent a more homogeneous population suitable for allogenic use. Emerging pre-clinical and clinical data however suggest similar, or even superior efficacy of ADRCs as compared to ASCs for indications involving (micro)vascular deficiency. Since CD31+ ADRCs lack in cultured ASCs, we hypothesized that these cells account for improvement of vascular function in the heterogenous ADRCs. Herein, we found that in patients with erectile dysfunction (ED), the number of injected CD31+ ADRCs correlates positively with erectile function 12 months after one bolus of autologous ADRCs. Comprehensive in vitro and ex vivo analyses confirmed superior pro-angiogenic and paracrine effects of human CD31+ enriched ADRCs compared to the corresponding CD31- and parent ADRCs. CD31+, CD31- and ADRCs were co-cultured in aortic ring-, as well as in ED-relevant corpus cavernousum tube formation assays, both showing a significantly higher ability of the CD31+ ADRCs to support tube development. This effect was corroborated using conditioned medium (CM), while quantitative mass spectrometric analysis suggested that this is explained by secretory pro-angiogenic proteins such as DKK3, ANGPT2, ANAX2 and VIM, all being enriched in CD31+ADRC CM. To gain further specification of the ADRC subpopulations expressing these proteins, single-cell RNA sequencing was performed and showed that transcripts of the upregulated and secreted proteins were present in 9 endothelial ADRC subsets including endothelial progenitor cells in the heterogenous non-cultured ADRCs. Our data thus suggest that the vascular benefit of using ADRCs in regenerative medicine is dictated by CD31+ ADRCs, which likely represent an improved alternative to heterogenous ADRCs as well as ASCs when aiming for vascular repair in cell therapy.
HostingRepositoryPRIDE
AnnounceDate2024-10-22
AnnouncementXMLSubmission_2024-10-22_06:08:39.179.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterHans Christian Beck
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListTMT6plex-126 reporter+balance reagent acylated residue; deaminated residue
InstrumentOrbitrap Fusion Lumos
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-02-24 06:18:20ID requested
12023-10-24 11:09:08announced
22023-11-14 09:07:24announced2023-11-14: Updated project metadata.
32024-10-22 06:08:40announced2024-10-22: Updated project metadata.
Publication List
Dhumale P, Nielsen JV, Hansen ACS, Burton M, Beck HC, J, ø, rgensen MG, Toyserkani NM, Haahr MK, Hansen ST, Lund L, Thomassen M, S, ø, rensen JA, Andersen DC, Jensen CH, Sheikh SP, CD31 defines a subpopulation of human adipose-derived regenerative cells with potent angiogenic effects. Sci Rep, 13(1):14401(2023) [pubmed]
10.1038/s41598-023-41535-1;
Keyword List
submitter keyword: CD31, proteomics, regenerative cells
Contact List
Hans Christian Beck
contact affiliationProteomics Lab, Odense University Hospital, Odense DK
contact emailhans.christian.beck@rsyd.dk
lab head
Hans Christian Beck
contact affiliationOdense University Hospital, Odense, Denmark
contact emailhans.christian.beck@rsyd.dk
dataset submitter
Full Dataset Link List
Dataset FTP location
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PRIDE project URI
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